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Cardiac complications and iron overload in beta thalassemia major patients-a systematic review and meta-analysis
F Koohi1, T Kazemi2, E Miri-Moghaddam3
1Student Research Committee, Department of Epidemiology, School of Public Health and Safety, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Insights
Cardiac iron overload and heart disease are prevalent in thalassemia major patients. Early detection and iron chelation therapy are crucial for managing these cardiovascular complications in transfusion-dependent thalassemia.
Area of Science:
- Hematology
- Cardiology
- Public Health
Background:
- Thalassemia major management has improved, but iron overload remains a significant challenge.
- Cardiac disease is a leading cause of morbidity and mortality in thalassemia major patients.
- Understanding the global prevalence of cardiac complications is essential for patient care.
Purpose of the Study:
- To determine the worldwide prevalence of cardiac iron overload.
- To assess the prevalence of cardiovascular complications in transfusion-dependent thalassemia patients.
- To inform strategies for preventing and managing cardiac issues in this population.
Main Methods:
- A systematic review and meta-analysis of studies published up to February 2018.
- Databases searched included ISI/Web of Science, Embase, PubMed, and Scopus.
- Prevalence was calculated using a random-effects model (Metaprop) on data from 142 studies with 26,893 patients.
Main Results:
- The overall prevalence of cardiac iron overload (myocardial siderosis, T2* < 20 ms) was 25% (95% CI 22-28%).
- The overall prevalence of cardiac complications was 42% (95% CI 37-46%).
- These findings indicate a high prevalence of cardiac issues in thalassemia major.
Conclusions:
- Cardiac iron overload and cardiovascular complications are highly prevalent in thalassemia major.
- Effective iron chelation therapy and regular monitoring of serum ferritin are vital.
- Echocardiography and electrocardiography aid in the early detection of cardiac complications in transfusion-dependent thalassemia (TDT) patients.
Abstract:
Despite the major improvement in therapeutic management of thalassemia major, iron overload is considered a challenging conundrum in these patients and heart disease still remains a major cause of morbidity and mortality in these patients. Therefore, this study aimed to investigate the prevalence of cardiac iron overload and cardiovascular complications in transfusion-dependent thalassemia patients in the worldwide. The following databases were searched: ISI/Web of Science, Embase, PubMed, Scopus, up to February 30, 2018. The quality of the studies was evaluated using the Joanna Briggs Institute Prevalence Critical Appraisal Tool. The random model based on Metaprop was used. One hundred forty-two studies were included. The total number of patients included was 26,893. The mean age of patients was 22.6 (SD = 1.7) years. Based on Metaprop, the overall prevalence of cardiac iron overload/myocardial sidoresis (T2* < 20 ms) and cardiac complications in thalassemia major patients in the worldwide was 25% (95% CI 22-28%) and 42% (95% CI 37-46%), respectively. The results of this study show that the prevalence of cardiac iron overload and cardiovascular complications in patients with thalassemia major is almost high. Therefore, iron chelation and careful monitoring of serum ferritin level will prevent the cardiac iron overload, and interval monitoring of patients with transfusion-dependent thalassemia (TDT) by echocardiography and electrocardiography will help with early detection of cardiovascular complications.
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